A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660265



Internal ID9926370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25535839..25536862hg38UCSC Ensembl
Outerchr11:25535682..25537015hg38UCSC Ensembl
Innerchr11:25557385..25558408hg19UCSC Ensembl
Outerchr11:25557228..25558561hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv196e199
Supporting Variantsessv5728996, essv6418366, essv5836594, essv6152427
SamplesHG00650, NA18605, NA18546, HG00478
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660265
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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